The position arranges and oversees all clinical trial activities and plays a key role in assisting the Principal Investigator (PI) in recruiting patients for clinical studies. The position works close...
read moreThe position arranges and oversees all clinical trial activities and plays a key role in assisting the Principal Investigator (PI) in recruiting patients for clinical studies. Combining state-of-the-a...
read moreThe position arranges and oversees all clinical trial activities and plays a key role in assisting the Principal Investigator (PI) in recruiting patients for clinical studies. The position works close...
read moreThe Clinical Research Associate will support clinical research activities within research sites that are actively participating in clinical trials. Under the direction of the Clinical Study Manager(s)...
read moreResponsible for providing Clinical Research support for all clinical trials. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to c...
read moreThe Clinical Research Associate will support clinical research activities within research sites that are actively participating in clinical trials. Under the direction of the Clinical Study Manager(s)...
read moreAssociate Director / Director Clinical Research Scientist - Remote (East Coast only)New York City Metropolitan AreaCompany: Biotech/Pharma companySummary:We are currently working with a client looking...
read moreEverest Clinical Research ("Everest") is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechn...
read moreSyndax Pharmaceuticals is looking for a Clinical Research Associate. Perform a key role in building relationships with site Clinical Coordinators, Study Investigators, and Service Provider partners an...
read moreResponsible for providing Clinical Research support for all clinical trials. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to c...
read moreThe Clinical Research Associate I monitors all aspects of clinical research trial(s) Clinical study life-cycle responsibilities including site management, ongoing maintenance and closure of pre-clinic...
read moreThe Clinical Research Associate I monitors all aspects of clinical research trial(s) Clinical study life-cycle responsibilities including site management, ongoing maintenance and closure of pre-clinic...
read moreAt least 2 years' experience as a Clinical Research Associate with a sound track record in managing clinical trial sites. Maintain current knowledge related to cancer therapy, clinical trial design an...
read moreAt least 2 years' experience as a Clinical Research Associate with a sound track record in managing clinical trial sites. Maintain current knowledge related to cancer therapy, clinical trial design an...
read moreAt least 4 years' experience as a Clinical Research Associate with a sound track record in managing clinical trial sites. Maintain current knowledge related to cancer therapy, clinical trial design an...
read moreAt least 4 years' experience as a Clinical Research Associate with a sound track record in managing clinical trial sites. Maintain current knowledge related to cancer therapy, clinical trial design an...
read moreThe Senior Clinical Research Associate (CRA) will act as a liaison between Ferring (the study Sponsor) and the sites/clinics that conduct their assigned clinical studies. Ensure site(s) maintains an a...
read moreThe Senior Clinical Research Associate (CRA) will act as a liaison between Ferring (the study Sponsor) and the sites/clinics that conduct their assigned clinical studies. Ensure site(s) maintains an a...
read moreResponsible for providing Clinical Research support for all clinical trials. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to c...
read moreIn depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, i. IQVIA is a leading global provider of clinical research services, commercial insights and healthc...
read moreResponsible for providing Clinical Research support for all clinical trials. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to c...
read moreIn depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, i. IQVIA is a leading global provider of clinical research services, commercial insights and healthc...
read moreResponsible for providing Clinical Research support for all clinical trials. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to c...
read moreAdvanced knowledge of Clinical investigation of medical devices for human subjects - Good Clinical Practice (ISO 14155), 21 CFR Part 11, 50, 54, 812 and other applicable regulations, fundamental knowl...
read moreResponsible for providing Clinical Research support for all clinical trials. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to c...
read moreResponsible for providing Clinical Research support for all clinical trials. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to c...
read moreResponsible for providing Clinical Research support for all clinical trials. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to c...
read moreInitiation / implementation of the observational or clinical research projects assigned including: Maintenance of Investigator and Research Staff CVs, Licensure and Training Records, Drafting and upda...
read moreAs a Sr CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Primary interfaces: Provider Functional Manager, Clinical T...
read moreAs a Sr CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Primary interfaces: Provider Functional Manager, Clinical T...
read moreWe’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development as a Clinical Research Associ...
read moreWorldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that a...
read moreIQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. If applicable, may be accountable for site financial manage...
read moreGood knowledge of, and skill in applying, applicable clinical research regulatory requirements. IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research ser...
read moreIQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. Good knowledge of, and skill in applying, applicable clinic...
read moreThe Cancer Clinical Trials Senior Research Associate supports the research team in the overall conduct of clinical trials using Good Clinical Practice. The Senior Research Associate can function indep...
read moreThe Cancer Clinical Trials Senior Research Associate supports the research team in the overall conduct of clinical trials using Good Clinical Practice. The Senior Research Associate can function indep...
read moreUnique opportunities exist for collaborations between clinical and research programs, including clinical trials research, cancer chemoprevention, clinical and basic pharmacology, and Phase 1 clinical ...
read moreAs a Clinical Research Associate (CRA) III, your responsibilities:. Clinical Research Associate (CRA) III. Strong knowledge of Good Clinical Practice (international quality standard for human clinical...
read moreClinical Research Associate (CRA) III. As a Clinical Research Associate (CRA) III, your responsibilities:. Strong knowledge of Good Clinical Practice (international quality standard for human clinical...
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